Home NDC 52000-072 Muscle Rub Pain Reliever Gel
Product NDC 52000-072
11-digit product format 520000072
Labeler code 52000
Product ID 52000-072_db1541b7-b2be-4751-a391-f0966f834ca3
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route TOPICAL
Labeler Universal Distribution Centre LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-24
Substance MENTHOL, UNSPECIFIED FORM
Active strength 25 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes NDC auxiliary status# Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table Dataset Scope Product NDC Package NDC Code Status Reporting period Source date excluded product product 52000-072 I Inactivated by FDA 2026-07-31 excluded package package 52000-072 52000-072-02 I Inactivated by FDA 2026-07-31
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings For external use only. Do not use on wounds or damaged skin with a heating pad on a child under 12 years of age with arthritis-like conditions Ask a doctor before use if you have redness over the affected area When using this product avoid contact with eyes or mucous membranes do not bandage tightly Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive skin irritation occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Additional Listing Data#
Finished product Yes
Brand name base Muscle Rub Pain Reliever Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 25 mg/g
Harmonized Identifiers# Field, Values table Field Values Unii L7T10EIP3A Rxcui 282805
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52000-072-01 Muscle Rub Pain Reliever Gel 35.4 g in 1 TUBE GEL 35.4 4 52000-072-02 Muscle Rub Pain Reliever Gel 1 in 1 CARTON GEL 1 4 52000-072-03 Muscle Rub Pain Reliever Gel 35.4 g in 1 TUBE GEL 35.4 3 52000-072-04 Muscle Rub Pain Reliever Gel 1 in 1 CARTON GEL 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52000-072 MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] 4 Current NDC, Legacy NDC, 2 package rows 20241212_b9a563b6-7988-79df-e053-2995a90a752b.zip 52000-072 MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] 2 Current NDC, Legacy NDC, 2 package rows 20241218_18536e21-afc3-8447-e063-6394a90aabae.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52000-072-01 52000007201 35.4 g in 1 TUBE 35.4 g Historical 52000-072-02 52000007202 1 TUBE in 1 CARTON (52000-072-02) > 35.4 g in 1 TUBE (52000-072-01) 1 tube 2021-01-24 0000-00-00 No No Current 52000-072-03 52000007203 35.4 g in 1 TUBE 35.4 g Historical 52000-072-04 52000007204 1 TUBE in 1 CARTON (52000-072-04) / 35.4 g in 1 TUBE (52000-072-03) 1 tube 2021-01-24 No No Current